NCT02586818撤回不适用
Clinical Performance of the Investigational InRhythm PT/INR System in a Professional Use Setting
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 主要终点
- Comparison of INR measurements
研究概览
简要总结
This study is designed to evaluate and verify the clinical accuracy of the InRhythm PT/INR system; a point-of-care, whole blood PT/INR measurement with a reference plasma based PT/INR using a laboratory reference instrument and reagent (Sysmex/lnnovin) calibrated to the WHO rTF09 reference standard.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Comparison of INR measurements
时间窗: 5 weeks
次要结局
未报告次要终点
研究者
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